Variant report

Variant	rs4698783
Chromosome Location	chr4:110668980-110668981
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10020460	1.00[ASW][hapmap];0.81[LWK][hapmap];0.93[YRI][hapmap];0.85[AFR][1000 genomes]
rs10049635	0.85[AFR][1000 genomes]
rs10856999	1.00[YRI][hapmap]
rs10857000	1.00[ASW][hapmap];0.88[LWK][hapmap];1.00[YRI][hapmap]
rs11098044	0.93[YRI][hapmap];0.83[AFR][1000 genomes]
rs11098045	1.00[YRI][hapmap]
rs11936921	0.93[YRI][hapmap];0.92[AFR][1000 genomes]
rs13152659	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs4382037	0.87[ASW][hapmap];0.81[LWK][hapmap];0.93[YRI][hapmap];0.83[AFR][1000 genomes]
rs62324897	0.81[AFR][1000 genomes]
rs6533458	1.00[YRI][hapmap]
rs6533459	1.00[YRI][hapmap]
rs7437142	0.87[ASW][hapmap];0.81[LWK][hapmap];0.93[YRI][hapmap];0.83[AFR][1000 genomes]
rs7439880	1.00[YRI][hapmap]
rs7441380	0.96[AFR][1000 genomes]
rs7674237	1.00[YRI][hapmap]
rs7683027	0.86[YRI][hapmap];0.83[AFR][1000 genomes]
rs7698552	0.96[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3349784	chr4:110348873-110723163	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv4463	chr4:110647731-110693125	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110651800-110669400	Weak transcription	Spleen	Spleen
2	chr4:110652000-110682800	Weak transcription	Left Ventricle	heart
3	chr4:110652000-110686000	Weak transcription	Ovary	ovary
4	chr4:110658000-110684000	Weak transcription	Duodenum Mucosa	Duodenum
5	chr4:110658800-110669800	Weak transcription	Pancreas	Pancrea
6	chr4:110659200-110689000	Weak transcription	Fetal Intestine Large	intestine
7	chr4:110662000-110672400	Strong transcription	HepG2	liver
8	chr4:110665000-110690400	Weak transcription	Fetal Intestine Small	intestine
9	chr4:110665800-110670000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr4:110666400-110670800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr4:110667600-110671800	Weak transcription	K562	blood
12	chr4:110667800-110669800	Genic enhancers	Liver	Liver
13	chr4:110668600-110671800	Weak transcription	Lung	lung

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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